A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3660764



Internal ID19032086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45335231..45335231hg38UCSC Ensembl
chr20:43963871..43963871hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16483891
Samples
Known GenesSDC4
MethodSequencing
Analysisde novo assemblies produced from SoapDenovo2 were aligned to GRC37 using LAST and input into SoapAsmVar for population-wide structural variation detection. The method is described in the publication
PlatformIllumina HiSeq 2000
Comments
ReferenceBesenbacher_et_al_2015
Pubmed ID25597990
Accession Number(s)esv3660764
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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